CNR Institutional Research Information System

D'ESPOSITO, MAURIZIO
 Distribuzione geografica
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Continente #
AS - Asia 2.472
NA - Nord America 1.224
EU - Europa 558
SA - Sud America 456
AF - Africa 59
Totale 4.769
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Nazione #
US - Stati Uniti d'America 1.168
SG - Singapore 1.081
CN - Cina 515
BR - Brasile 372
HK - Hong Kong 307
VN - Vietnam 233
FR - Francia 150
IT - Italia 136
KR - Corea 106
DE - Germania 69
NL - Olanda 63
BD - Bangladesh 45
IN - India 41
GB - Regno Unito 36
JP - Giappone 34
CA - Canada 29
AR - Argentina 24
FI - Finlandia 20
ZA - Sudafrica 19
MX - Messico 16
ID - Indonesia 15
IQ - Iraq 15
TR - Turchia 15
CL - Cile 13
EC - Ecuador 13
PL - Polonia 12
MA - Marocco 10
SA - Arabia Saudita 10
IL - Israele 9
PY - Paraguay 9
RU - Federazione Russa 9
UZ - Uzbekistan 9
CO - Colombia 8
VE - Venezuela 8
AT - Austria 7
ES - Italia 7
CZ - Repubblica Ceca 6
EG - Egitto 6
UA - Ucraina 6
GR - Grecia 5
LT - Lituania 5
PK - Pakistan 5
AZ - Azerbaigian 4
DZ - Algeria 4
IE - Irlanda 4
JO - Giordania 4
KE - Kenya 4
SE - Svezia 4
AE - Emirati Arabi Uniti 3
AL - Albania 3
BO - Bolivia 3
KZ - Kazakistan 3
MY - Malesia 3
TH - Thailandia 3
TN - Tunisia 3
BW - Botswana 2
CH - Svizzera 2
ET - Etiopia 2
GY - Guiana 2
HN - Honduras 2
HU - Ungheria 2
KG - Kirghizistan 2
KW - Kuwait 2
LB - Libano 2
PE - Perù 2
RO - Romania 2
RS - Serbia 2
UY - Uruguay 2
ZM - Zambia 2
AM - Armenia 1
AO - Angola 1
BE - Belgio 1
BG - Bulgaria 1
CG - Congo 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GD - Grenada 1
GT - Guatemala 1
HR - Croazia 1
JM - Giamaica 1
KH - Cambogia 1
LV - Lettonia 1
MD - Moldavia 1
ML - Mali 1
MM - Myanmar 1
MU - Mauritius 1
NG - Nigeria 1
NI - Nicaragua 1
PH - Filippine 1
PS - Palestinian Territory 1
PT - Portogallo 1
SC - Seychelles 1
SI - Slovenia 1
SV - El Salvador 1
TC - Turks e Caicos 1
TJ - Tagikistan 1
TT - Trinidad e Tobago 1
Totale 4.769
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Città #
Singapore 648
Santa Clara 376
Hong Kong 303
Hefei 211
San Jose 130
Lauterbourg 115
Seoul 103
Ho Chi Minh City 101
Ashburn 94
Beijing 87
Los Angeles 83
Hanoi 54
Frankfurt am Main 44
Naples 33
São Paulo 32
Dallas 31
Buffalo 25
New York 25
Tokyo 20
Rome 16
Avellino 13
Curitiba 12
Orem 12
Rio de Janeiro 12
Turners Falls 11
Atlanta 10
Aversa 10
Brooklyn 10
Helsinki 10
Minamishinagawa 10
Haiphong 9
Montreal 9
Tashkent 9
Baghdad 8
Chennai 8
Da Nang 8
Guangzhou 8
Johannesburg 8
London 8
Manchester 8
Brasília 7
Campinas 7
Dhaka 7
Fortaleza 7
Milan 7
San Francisco 7
Toronto 7
Warsaw 7
Amsterdam 6
Belo Horizonte 6
Denver 6
Jeddah 6
Munich 6
Phoenix 6
Turku 6
Athens 5
Cairo 5
Chicago 5
Cleveland 5
Istanbul 5
Malang 5
Porto Alegre 5
Redondo Beach 5
Amman 4
Asunción 4
Baku 4
Bengaluru 4
Boston 4
Cape Town 4
Dublin 4
Düsseldorf 4
Elk Grove Village 4
Franca 4
Goiânia 4
Guayaquil 4
Karachi 4
Lappeenranta 4
Mauá 4
Nairobi 4
Newark 4
Ninh Bình 4
Osasco 4
Quảng Ngãi 4
Santiago 4
Stockholm 4
Teresina 4
Vienna 4
Betim 3
Bologna 3
Buenos Aires 3
Bắc Ninh 3
Campos dos Goytacazes 3
Caracas 3
Casablanca 3
Caxias do Sul 3
Divinópolis 3
Hanover 3
Juazeiro do Norte 3
Kyoto 3
Maceió 3
Totale 2.997
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Nome #
Epigenetic control of hypoxia inducible factor-1?-dependent expression of placental growth factor in hypoxic conditions 101
X inactivation and reactivation in X-linked diseases 93
F(2)-dihomo-isoprostanes as potential early biomarkers of lipid oxidative damage in Rett syndrome 79
Multi-omics data integration provides insights into the post-harvest biology of a long shelf-life tomato landrace 72
F(4)-neuroprostanes mediate neurological severity in Rett syndrome. 68
Glycosphingolipid metabolic reprogramming drives neural differentiation 66
MULTI-OMICS ANALYSIS SHEDS LIGHT ON HOW SHELF-LIFE OF TOMATO FRUIT IS PROLONGED 65
The evolutionary history of the second pseudoautosomal region revised 64
Genomic and epigenomic analysis of tomato fruit senescence 61
Select item 10671Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. Online. 60
Agonist stimulated 5-HT7R recovers gene expression profile in cortical neurons of a Rett syndrome mouse model 59
GENOME-WIDE ANALYSIS OF HISTONE MODIFICATIONS AND ASSOCIATION WITH RIPENING-RELATED GENES DURING POST-HARVEST IN TOMATO FRUIT 57
Alternative splicing of the human gene SYBL1 modulates protein domain architecture of longin VAMP7/TI-VAMP, showing both non-SNARE and synaptobrevin-like isoforms. 57
Minimally Invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples. 55
Global transcriptome profiles of italian mediterranean buffalo embryos with normal and retarded growth. 55
Genetic variability at the second pseudoautosomal region in ancient and modern humans 55
INSIGHTS INTO FRUIT SENESCENCE REGULATORY NETWORKS IN A TOMATO LANDRACE WITH LONG SHELF-LIFE 54
DNA methylation in X inactivation, imprinting and associated diseases 53
A dual mechanism controlling the localization and function of exocytic v-SNAREs 53
Transcriptomic and epigenomic landscape in rett syndrome 52
ZFP57/KAP1 Genomic Association and Targeted Epigenetic Regulation at Imprinted and Not Imprinted Loci 52
Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome 52
A Multi-Omics approach to get insights into fruit senescence regulatory networks in a tomato landrace with long shelf-life. 52
CODING AND NON-CODING RNAS IN A LONG SHELF-LIFE TOMATO VARIETY 52
Effects of Mecp2 loss of function in embryonic cortical neurons: a bioinformatics strategy to sort out non-neuronal cells variability from transcriptome profiling 52
O6-methylguanine-DNA methyltransferase in equine sarcoids: molecular and epigenetic analysis. 51
MECP2, a multi-talented modulator of chromatin architecture 51
In vivo analysis of DNA methylation patterns recognized by specific proteins: coupling chromatin immunoprecipitation and bisulfite genomic sequencing 50
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 49
Deep Insights Into Mecp2-Driven Transcriptional (De)Regulation At Embryonic Developmental Stage Through RNA-Seq Data Analysis 49
Vamp7 46
The X-linked methyl binding protein gene Kaiso is highly expressed in brain but is not mutated in Rett syndrome patients 46
Early oxidative damage in Rett mouse brain 45
Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome 45
Multi-Omics analysis of tomato fruit senescence 45
Genomic characterization and chromosomal mapping of 5 river buffalo skeletal muscle differentiation master genes 44
Human synaptobrevin like 1 gene basal transcription is regulated through the interaction of Staf-ZNF143 factors with evolutionary conserved Cis-elements 43
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing. 43
Reduced brain UCP2 expression mediated by microRNA-503 contributes to increased stroke susceptibility in the high-salt fed stroke-prone spontaneously hypertensive rat 42
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome 42
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 42
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 41
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 41
Defective Sphingosine-1-phosphate metabolism is a druggable target in Huntington's disease. 40
Epigenetic regulation of hypoxia-induced PlGF expression 39
Non-coding RNAs in chromatin disease involving neurological defects 39
Differential DNA Methylation as a Tool for Non-Invasive Prenatal Diagnosis (NIPD) of X Chromosome Aneuploidies 39
Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region 38
Expressed STSs and transcription of human Xq28. 37
From sequence analysis to diseases identification in the distal human xq28 37
Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome 37
Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia. 37
Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modifications 36
VAMP subfamilies identified by specific R-SNARE motifs 36
An autoregulatory loop mediated by miR-21 and PDCD4 controls the AP-1 activity in RAS transformation 36
MECP2 Duplication Syndrome: Evidence of Enhanced Oxidative Stress. A Comparison with Rett Syndrome 36
Molecular and epigenetic analysis of the fragile histidine triad tumour suppressor gene in equine sarcoids 36
Anti-Mullerian hormone (AMH) concentration in follicular fluid and mRNA expression of AMH receptor type II and LH receptor in granulosa cells as predictive markers of good buffalo (Bubalus bubalis) donors 35
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 35
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome. 34
Longins and their longins domains:regulated SNAREs and multifunctional SNARE regulators 34
Expression of HOX homeogenes in human neuroblastoma cell culture lines. 33
Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples 32
Chromosome territory re-organisation in a human disease with altered DNA methylation 32
Complex Events In The Evolution Of The Human Pseudoautosomal Region 2 (PAR2) 32
Molecular analysis of the heterogeneity region of the human ribosomal spacer. 32
Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes. 32
The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice site. 32
Partial rescue of Rett syndrome by omega-3 polyunsaturated fatty acids (PUFAs) oil 31
Role of Mecp2 in the High-Order Chromatin Structure During Neural Differentiation 31
Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease 31
Relationships between MeCP2 and pericentric heterochromatin factors during neural differentiation 31
Gene Expression Profile in Liver Transplantation and the Influence of Gene Dysregulation Occurring in Deceased Donor Grafts 31
Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modifications 30
Expression of HOX homeogenes in human neuroblastoma cell culture lines 30
4. Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 30
MeCP2 as a genome-wide modulator: the renewal of an old story. 30
Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotype. 29
Chapter 18. Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples. 29
Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome 29
Partial rescue of Rett syndrome by omega-3 polyunsaturated fatty acids (PUFAs) oil 28
DDX11L: a novel transcript family emerging from human subtelomeric regions 28
Epigenetic control of hypoxia-induced Placental Growth Factor expression 28
MeCP2 transcription analysis and X-inactivation pattern in a Rett girl brain tissue. 27
Two human homeobox genes. c1 and c8: structure analysis and expression in embryonic development. 27
Physical mappaing of a retinal-specific trascription factor and the epigenetic mark H3K9me3 correlated to rhodopsin and genome wide retinal loci. 27
Second Human Peudoautosomal Region: Biology, Genes and Implication for the Pathogenesis of Rett Syndrome 27
DNA methylation 40 years later: its role in human health and disease 27
Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome. 27
DNA METHYLATION IN TRANSCRIPTIONAL REPRESSION OF TWO DIFFERENTIALLY EXPRESSED X-LINKED GENES, GPC3 AND SYBL1 27
Molecular dissection of two human chromatin disease, Rett syndrome and ICF syndrome 27
Involvement of HIF-1alfa in hypoxia-induced Placental Growth Factor expression 26
Epigenomic and transcriptional effects of Dnmt3b mutations in human ICF syndrome-derived B cell lines. 26
Scavenger Receptor B1 oxidative post-translational modifications are responsible for its loss in Rett syndrome 26
EPITOM: an integrated study of epigenomics in tomato fruit during post-harvest 26
A serine 37 mutation associated with two missense mutations at highly conserved regions of p53 affect pro-apoptotic genes expression in a T-lymphoblastoid drug resistant cell line 26
Molecular cloning and characterization of the clock gene period2 in the testis of lizard Podarcis sicula and its expression during seasonal reproductive cycle 25
MeCP2 is required for major satellite forward transcript recruitment at pericentric heterochromatin during neural differentiation 25
null 25
Absence of TI-VAMP/Vamp7 Leads to Increased Anxiety in Mice. 25
Totale 4.132
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Categoria #
all - tutte 15.623
article - articoli 11.056
book - libri 68
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 426
Totale 27.173
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202431 0 0 0 0 0 0 0 0 2 0 28 1
2024/20251.810 32 9 150 75 347 51 8 88 51 80 494 425
2025/20262.943 157 256 278 474 525 167 472 150 147 179 138 0
Totale 4.784